Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Annukka M. Lahtinen"'
Autor:
Laura Ollila, Johanna Kuusisto, Keijo Peuhkurinen, Satu Kärkkäinen, Petri Tuomainen, Maija Kaartinen, Olayinka Raheem, Bjarne Udd, Jarkko Magga, Janne Rapola, Annukka M. Lahtinen, Eero Lehtonen, Miia Holmström, Sari Kivistö, Elisabeth Widén, Markku Saksa, Tiina Heliö
Publikováno v:
Cardiogenetics, Vol 3, Iss 1, Pp e1-e1 (2013)
LMNA mutations are amongst the most important causes of familial dilated cardiomyopathy. The most important cause of arrhythmogenic right ventricular cardiomyopathy (ARVC) is desmosomal pathology. The aim of the study was to elucidate the role of LMN
Externí odkaz:
https://doaj.org/article/1ac03474f93c4cf9817d65b3387c2ae0
Autor:
Kirsi Penttinen, Heikki Swan, Sari Vanninen, Jere Paavola, Annukka M Lahtinen, Kimmo Kontula, Katriina Aalto-Setälä
Publikováno v:
PLoS ONE, Vol 10, Iss 7, p e0134746 (2015)
Externí odkaz:
https://doaj.org/article/45d3c1ae22744b7b937b6dc99812d561
Autor:
Annukka M Lahtinen, Peter A Noseworthy, Aki S Havulinna, Antti Jula, Pekka J Karhunen, Johannes Kettunen, Markus Perola, Kimmo Kontula, Christopher Newton-Cheh, Veikko Salomaa
Publikováno v:
PLoS ONE, Vol 7, Iss 7, p e41675 (2012)
Sudden cardiac death (SCD) accounts for up to half of cardiac mortality. The risk of SCD is heritable but the underlying genetic variants are largely unknown. We investigated whether common genetic variants predisposing to arrhythmia or related elect
Externí odkaz:
https://doaj.org/article/56ac27cae07448f7a13a2a13117a27a0
Autor:
Annukka M. Lahtinen, Kimmo Kontula, Jaakko T. Leinonen, Heikki Swan, Annukka Marjamaa, Hugues Abriel, Mohamed Yassine Amarouch, Elisabeth Widen, Lauri Toivonen
Publikováno v:
Annals of Noninvasive Electrocardiology. 21:343-351
Background The cardiac sodium channel Nav1.5, encoded by the gene SCN5A, is associated with a wide spectrum of hereditary arrhythmias. The gain-of-function mutation p.I141V in SCN5A was identified in a large multigenerational family with exercise-ind
Autor:
Yuki Bradford, Toshiko Tanaka, Jeffrey R. O'Connell, Florence Kyndt, Unnur Thorsteinsdottir, Ivana Kolcic, Xiaoyan Yin, Vincent Probst, Manolis Kellis, Christopher Newton-Cheh, Stefan Kääb, Argelia Medeiros-Domingo, Markus M. Nöthen, Paolo Gasparini, Jean-Jacques Schott, Ruth J. F. Loos, Thomas W. Mühleisen, Annukka Marjamaa, Morris Brown, Igor Rudan, Runjun D. Kumar, Peter J. Schwartz, Lars Lind, Martina Müller-Nurasyid, Xinchen Wang, Joshua C. Denny, Roberto Insolia, Soumya Raychaudhuri, Stephen W. Scherer, Bruno H. Stricker, Alexander Kluttig, Adamo Pio D'Adamo, Laurie A. Boyer, Moritz F. Sinner, Norbert Frey, Nour Eddine El Mokhtari, Thomas Meitinger, Jesper V. Olsen, Gerjan Navis, Steven R. Cummings, Richard W Morris, Nynke Hofman, Marcel den Hoed, Rudolf A. de Boer, Gonçalo R. Abecasis, Mark J. Daly, Dan M. Roden, Christian Gieger, Lyudmyla Kedenko, Marcus Dörr, Thomas P. Cappola, Afshin Parsa, Kari Stefansson, Markus Perola, Mark Eijgelsheim, Fredrik Nyberg, Robert M. Hamilton, Yalda Jamshidi, W. H. Linda Kao, Terho Lehtimäki, Annette Peters, David Schlessinger, Peter P. Pramstaller, James F. Wilson, Vilmundur Gudnason, Florian Kronenberg, Aroon D. Hingorani, Connie R. Bezzina, Abdennasser Bardai, Marylyn D. Ritchie, Andrew S. Plump, Johan Sundström, Daryl Waggott, Chrysoula Dalageorgou, Paul I.W. de Bakker, Uwe Völker, Aaron Isaacs, Oscar H. Franco, Yongmei Liu, Andrew N. Nicolaides, Lia Crotti, Cornelia M. van Duijn, Ben A. Oostra, Arne Pfeufer, Karl Werdan, Michael Morley, Jan A. Kors, Julien Barc, Lewin Eisele, Siegfried Perz, Stéphanie Chatel, Pieter A. van der Vleuten, Sara L. Pulit, Anna F. Dominiczak, Harry Campbell, Alice Ghidoni, Irene Mateo Leach, Nona Sotoodehnia, Nina Mononen, Henriette E. Meyer zu Schwabedissen, Alvaro Alonso, Fabiola Del Greco M, Dan E. Arking, Vera Adamkova, Mike A. Nalls, Valur Emilsson, Edward G. Lakatta, Kirill Tarasov, Alan F. Wright, Lenore J. Launer, Erik Ingelsson, Karin Halina Greiser, Ozren Polasek, Massimo Carella, Daniel F. Gudbjartsson, Bouwe P. Krijthe, Hanna Prucha, Per Hoffmann, Maura Griffin, Stefan Kiechl, Angel Carracedo, Ilja M. Nolte, Christine E. Moravec, Johann Willeit, Joshua C. Bis, Patricia B. Munroe, Marcello Ricardo Paulista Markus, Hailiang Huang, Mika Kähönen, Albert Hofman, Peter H. Whincup, Dirk J. van Veldhuisen, Michael Knoflach, Alicia Lundby, Serena Sanna, Hagen Kälsch, Bernhard Paulweber, Kamil Slowikowski, Luigi Ferrucci, Melanie Waldenberger, Marco Bobbo, Annukka M. Lahtinen, Ann-Christine Syvänen, J. Gustav Smith, Åsa Torinsson Naluai, Jaroslav A. Hubacek, Jeffrey Brandimarto, Wendy S. Post, Lude Franke, Mark J. Caulfield, Folkert W. Asselbergs, André G. Uitterlinden, Stefan Gustafsson, Pim van der Harst, David J. Tester, David S. Siscovick, David O. Arnar, Sarah H Wild, Elizabeth J. Rossin, Albert V. Smith, Bruce M. Psaty, Georg Ehret, Alan R. Shuldiner, Stephen Newhouse, Kimmo Kontula, Maria Brion, Andre Franke, Peter W. Macfarlane, Mika Kivimäki, Tamara B. Harris, Lasse Oikarinen, Tamara T. Koopmann, Kenneth B. Margulies, Aravinda Chakravarti, Gianfranco Sinagra, Maarten P. van den Berg, Veikko Salomaa, Karl-Heinz Jöckel, Daniel S. Evans, Caroline Hayward, Kimmo Porthan, Michael J. Ackerman, Jacqueline C.M. Witteman, Arthur A.M. Wilde, Martin G. Larson, Kasper Lage, Manuela Uda, Susan R. Heckbert, Joel S. Bader, Graham Watt, María Dolores Torres, Stephan B. Felix, Jerome I. Rotter, Pau Navarro, Meena Kumari, Johan Ärnlöv, Andrew D. Paterson, Antti Jula, Olli T. Raitakari, Raimund Erbel, Christopher J. O'Donnell, Britt M. Beckmann, Peter A. Noseworthy, Tim D. Spector, Wai K. Lee, Leopoldo Zelante, Nilesh J. Samani, John R. Giudicessi, Harold Snieder, Dag S. Thelle, David Ellinghaus, Eimo Martens, James B. Strait, Jorma S. A. Viikari, Andrew D. Johnson, Antonella Mulas, Hilma Holm, Johannes Haerting, Annamaria Iorio, Rebecca L. Zuvich, Sheila Ulivi, Andrew A. Hicks, Elijah R. Behr, Leo-Pekka Lyytikäinen, Bernhard Strohmer, Marco Orru, Claudia Lamina, Sandosh Padmanabhan, Christian Fuchsberger, Andrie G. Panayiotou
Publikováno v:
Nature Genetics, 46(8), 826-36. Nature Publishing Group
Nature Genetics, Vol. 46, No 8 (2014) pp. 826-836
Nature Genetics, 46(8), 826-836. Nature Publishing Group
Nature genetics, 46(8), 826-836. Nature Publishing Group
Nature genetics
Nature Genetics, Vol. 46, No 8 (2014) pp. 826-836
Nature Genetics, 46(8), 826-836. Nature Publishing Group
Nature genetics, 46(8), 826-836. Nature Publishing Group
Nature genetics
The QT interval, an electrocardiographic measure reflecting myocardial repolarization, is a heritable trait. QT prolongation is a risk factor for ventricular arrhythmias and sudden cardiac death (SCD) and could indicate the presence of the potentiall
Autor:
Carla Spazzolini, Thomas Meitinger, Althea Goosen, Marshall Heradien, Gianfranco Parati, Peter J. Schwartz, Caterina Morassutto, Paul A. Brink, Elisa Mastantuono, Heikki Swan, Annukka M. Lahtinen, Peter Lichtner, Kimmo Kontula, Mari Cristina A Monti, Lia Crotti
We welcome the opportunity to respond to the expected comments by Amin et al regarding our article on the modifying role of 3′ untranslated region (3′UTR) single-nucleotide polymorphisms (SNPs) in type 1 long-QT syndrome patients.1 In the origina
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1adc902dc4611b98cc694af022a8b575
http://hdl.handle.net/10281/148488
http://hdl.handle.net/10281/148488
Autor:
Lia Crotti, Althea Goosen, Heikki Swan, Paul A. Brink, Marshall Heradien, Kimmo Kontula, Elisa Mastantuono, Peter J. Schwartz, Caterina Morassutto, Gianfranco Parati, Annukka M. Lahtinen, Thomas Meitinger, Maria Cristina Monti, Peter Lichtner, Carla Spazzolini
Background— Long-QT syndrome is an inherited cardiac channelopathy characterized by delayed repolarization, risk of life-threatening arrhythmia, and significant clinical variability even within families. Three single-nucleotide polymorphisms (SNPs)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a6427bb92b381e9ed78386590987a32
http://hdl.handle.net/10281/131754
http://hdl.handle.net/10281/131754
Autor:
Anita Hiippala, Annukka Marjamaa, Kimmo Kontula, Bianca Arrhenius, Lauri Toivonen, Heikki Swan, Juha-Matti Happonen, Annukka M. Lahtinen
Publikováno v:
Journal of Cardiovascular Electrophysiology. 23:194-199
Epinephrine Infusion in Diagnosis of CPVT. Introduction: A test involving intravenous infusion of epinephrine has been proposed as a method alternative to exercise stress test in diagnosis of catecholaminergic polymorphic ventricular tachycardia (CPV
Autor:
Annukka M. Lahtinen, Kimmo Kontula, Veli-Pekka Lehto, Annukka Lehtonen, Elisabeth Widen, Maija Kaartinen, Lauri Toivonen, Heikki Swan, Eero Lehtonen
Publikováno v:
International Journal of Cardiology. 126:92-100
Background Arrhythmogenic right ventricular dysplasia/cardiomyopathy (ARVD/C) is an inherited cardiac disorder characterized by life-threatening ventricular arrhythmias and fibrofatty replacement of myocardial tissue. Recent data suggest a dominant m
Autor:
Sari U. M. Vanninen, Kimmo Kontula, Katriina Aalto-Setälä, Jere Paavola, Kirsi Penttinen, Heikki Swan, Annukka M. Lahtinen
Publikováno v:
PLoS ONE
PLoS ONE, Vol 10, Iss 5, p e0125366 (2015)
PLoS ONE, Vol 10, Iss 5, p e0125366 (2015)
Catecholaminergic polymorphic ventricular tachycardia (CPVT) is a highly malignant inherited arrhythmogenic disorder. Type 1 CPVT (CPVT1) is caused by cardiac ryanodine receptor (RyR2) gene mutations resulting in abnormal calcium release from sarcopl